105 related articles for article (PubMed ID: 21475347)
21. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease].
Priora U; Quaglia P; Vivalda M; Giachino-Amistà MT; Domeneghetti G; Sardi R
Minerva Pediatr; 1987 Sep; 39(17-18):709-14. PubMed ID: 3437861
[No Abstract] [Full Text] [Related]
22. [Juvenile asymmetrical segmental spinal muscular atrophy].
Ørngreen MC; Gideon P; Pedersen HB; Olsen DB; Vissing J
Ugeskr Laeger; 2002 Aug; 164(35):4073-5. PubMed ID: 12229308
[TBL] [Abstract][Full Text] [Related]
23. [Infantile spinal muscular atrophy. An unusual disease with various differential diagnoses].
Solders G
Lakartidningen; 1993 Jan; 90(4):268-9. PubMed ID: 8433607
[No Abstract] [Full Text] [Related]
24. Atypical presentations of spinal muscular atrophy type III (Kugelberg-Welander disease).
Kang PB; Krishnamoorthy KS; Jones RM; Shapiro FD; Darras BT
Neuromuscul Disord; 2006 Aug; 16(8):492-4. PubMed ID: 16797181
[TBL] [Abstract][Full Text] [Related]
25. [Infantile spinal muscular atrophy type 1 mimicking axonal sensory-motor polyneuropathy].
Martín Fernández-Mayoralas D; Fernández-Jaén A; Nevado-Jiménez C; Muñoz-Jareño N; Vegas-Muñoz E; Calleja-Pérez B
Rev Neurol; 2009 Jun 16-30; 48(12):666-7. PubMed ID: 19507128
[No Abstract] [Full Text] [Related]
26. What They Don't See.
Clemens CM
Health Commun; 2018 Sep; 33(9):1194-1197. PubMed ID: 28678538
[TBL] [Abstract][Full Text] [Related]
27. Graves' hyperthyroidism following primary hypothyroidism due to Hashimoto's thyroiditis in a case of thyroid hemiagenesis: case report.
Ruchała M; Szczepanek E; Skiba A; Czepczyński R; Sowiński J
Neuro Endocrinol Lett; 2008 Feb; 29(1):55-8. PubMed ID: 18283259
[TBL] [Abstract][Full Text] [Related]
28. The use of invasive ventilation is appropriate in children with genetically proven spinal muscular atrophy type 1: the motion against.
Ryan MM
Paediatr Respir Rev; 2008 Mar; 9(1):51-4; discussion 55-6. PubMed ID: 18280980
[TBL] [Abstract][Full Text] [Related]
29. [Atypical celiac disease in a patient with type 1 diabetes mellitus and Hashimoto's thyreoiditis].
Schreiber FS; Ziob T; Vieth M; Elsbernd H
Dtsch Med Wochenschr; 2011 Jan; 136(3):82-5. PubMed ID: 21225554
[TBL] [Abstract][Full Text] [Related]
30. Association of oral lichen planus with thyroid disease in a Finnish population: a retrospective case-control study: "A different finding from a Mediterranean area".
Compilato D; Paderni C; Di Fede O; Gulotta G; Campisi G
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2011 Jan; 111(1):12-3; author reply 13-4. PubMed ID: 21176818
[No Abstract] [Full Text] [Related]
31. Four patients with hypothyroid Graves' disease.
Starrenburg-Razenberg AJ; Castro Cabezas M; Gan IM; Njo TL; Rietveld AP; Elte JW
Neth J Med; 2010 Apr; 68(4):178-80. PubMed ID: 20421660
[TBL] [Abstract][Full Text] [Related]
32. [Spinal muscular atrophy in young infants].
Smit LM; Hageman EG
Tijdschr Kindergeneeskd; 1989 Jun; 57(3):102-6. PubMed ID: 2799798
[TBL] [Abstract][Full Text] [Related]
33. [Very severe spinal muscular atrophy--type 0. A cause of congenital multiple arthrogryposis].
Balslev T; Hertz JM; Rackauskaite G; Sørensen LA
Ugeskr Laeger; 2001 Oct; 163(41):5679-80. PubMed ID: 11665473
[TBL] [Abstract][Full Text] [Related]
34. Clinical and molecular diagnosis of spinal muscular atrophy.
Panigrahi I; Kesari A; Phadke SR; Mittal B
Neurol India; 2002 Jun; 50(2):117-22. PubMed ID: 12134171
[TBL] [Abstract][Full Text] [Related]
35. [Adynamia, finger paresthesias].
Kraft K; Vetter H
Schweiz Rundsch Med Prax; 1989 Mar; 78(10):270-2. PubMed ID: 2704923
[TBL] [Abstract][Full Text] [Related]
36. A Curious Case of Acute Onset Bilateral Hand Weakness in a Youth Hockey Player: A Case Report.
Sherrier M; Miknevich MA
Am J Phys Med Rehabil; 2020 Jul; 99(7):656-659. PubMed ID: 31688010
[No Abstract] [Full Text] [Related]
37. Altered axonal excitability properties in juvenile muscular atrophy of distal upper extremity (Hirayama disease).
Sawai S; Misawa S; Kanai K; Isose S; Shibuya K; Noto Y; Fujimaki Y; Sekiguchi Y; Nasu S; Nomura F; Kuwabara S
Clin Neurophysiol; 2011 Jan; 122(1):205-9. PubMed ID: 20624687
[TBL] [Abstract][Full Text] [Related]
38. A newborn infant with infantile spinal muscular atrophy associated with trisomy 21 and congenital hypothyroidism.
Gulcan H; Uzum I; Dayangac D; Gurses I
Genet Couns; 2005; 16(1):113-4. PubMed ID: 15844790
[No Abstract] [Full Text] [Related]
39. [Juvenile muscular atrophy of unilateral upper extremity (Hirayama disease)--half-century progress and establishment since its discovery].
Hirayama K
Brain Nerve; 2008 Jan; 60(1):17-29. PubMed ID: 18232329
[TBL] [Abstract][Full Text] [Related]
40. Spinal muscular atrophy with respiratory distress type 1 (SMARD1).
Kaindl AM; Guenther UP; Rudnik-Schöneborn S; Varon R; Zerres K; Schuelke M; Hübner C; von Au K
J Child Neurol; 2008 Feb; 23(2):199-204. PubMed ID: 18263757
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
